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New Insight into the Reactivity of S,S-Bis-ylide.
Authesserre, Ugo; Swamy, V S V S N; Saffon-Merceron, Nathalie; Baceiredo, Antoine; Kato, Tsuyoshi; Maerten, Eddy.
Afiliação
  • Authesserre U; Université de Toulouse, UPS, and CNRS, LHFA UMR 5069, 118 Route de Narbonne, 31062 Toulouse, France.
  • Swamy VSVSN; Université de Toulouse, UPS, and CNRS, LHFA UMR 5069, 118 Route de Narbonne, 31062 Toulouse, France.
  • Saffon-Merceron N; Université de Toulouse, UPS, and CNRS, ICT UAR2599 118 Route de Narbonne, 31062 Toulouse, France.
  • Baceiredo A; Université de Toulouse, UPS, and CNRS, LHFA UMR 5069, 118 Route de Narbonne, 31062 Toulouse, France.
  • Kato T; Université de Toulouse, UPS, and CNRS, LHFA UMR 5069, 118 Route de Narbonne, 31062 Toulouse, France.
  • Maerten E; Université de Toulouse, UPS, and CNRS, LHFA UMR 5069, 118 Route de Narbonne, 31062 Toulouse, France.
Molecules ; 28(8)2023 Apr 07.
Article em En | MEDLINE | ID: mdl-37110528
The present work focuses on the reactivity of S,S-bis-ylide 2, which presents a strong nucleophilic character, as evidenced by reactions with methyl iodide and CO2, affording C-methylated salts 3 and betaine 4, respectively. The derivatization of betaine 4 affords the corresponding ester derivative 6, which is fully characterized by using NMR spectroscopy and X-ray diffraction analysis. Furthermore, an original reaction with phosphenium ions leads to the formation of a transient push-pull phosphino(sulfonio)carbene 8, which rearranges to give stabilized sulfonium ylide derivative 7.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Molecules Assunto da revista: BIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França